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1.
Orphanet J Rare Dis ; 19(1): 273, 2024 Jul 20.
Artigo em Inglês | MEDLINE | ID: mdl-39033298

RESUMO

BACKGROUND: Transthyretin amyloidosis (ATTR) is a multisystem disease caused by the deposition of fibrillar protein in organs and tissues. ATTR genotypes and phenotypes are highly heterogeneous. We present data on physical signs and symptoms, cardiac and neurological assessments and genetic profile of patients enrolled in the Transthyretin Cardiac Amyloidosis Registry of the State of São Paulo, Brazil. RESULTS: Six hundred-forty-four patients were enrolled, 505 with the variant form (ATTRv) and 139 with wild-type (ATTRwt). Eleven different mutations were detected, the most common being Val50Met (47.5%) and V142Ile (39.2%). Overall, more than half of the patients presented cardiac involvement, and the difference in this proportion between the ATTRv and ATTRwt groups was significant (43.9 vs. 89.9%; p < 0.001). The prevalence of the neurological phenotype also differed between ATTRv and ATTRwt (56.8 vs. 31.7%; p < 0.001). The mixed phenotype was found in 25.6% of the population, without a significant difference between ATTRv and ATTRwt groups. A group of patients remained asymptomatic (10.4%), with a lower proportion of asymptomatic ATTRwt patients. CONCLUSIONS: This study details the clinical and genetic spectrum of patients with ATTR in São Paulo, Brazil. This preliminary analysis highlights the considerable phenotypic heterogeneity of neurological and cardiac manifestations in patients with variant and wild-type ATTR.


Assuntos
Neuropatias Amiloides Familiares , Pré-Albumina , Humanos , Neuropatias Amiloides Familiares/genética , Neuropatias Amiloides Familiares/patologia , Brasil , Masculino , Feminino , Pessoa de Meia-Idade , Idoso , Pré-Albumina/genética , Pré-Albumina/metabolismo , Mutação/genética , Sistema de Registros , Adulto , Genótipo , Fenótipo
2.
Arq. bras. cardiol ; 121(7): e20240478, jun.2024. tab, graf
Artigo em Português | LILACS-Express | LILACS | ID: biblio-1568801
3.
Fernandes, Fabio; Simões, Marcus V; Correia, Edileide de Barros; Marcondes-Braga, Fabiana Goulart; Filho, Otavio Rizzi Coelho; Mesquita, Cláudio Tinoco; Mathias Junior, Wilson; Antunes, Murillo de Oliveira; Arteaga-Fernández, Edmundo; Rochitte, Carlos Eduardo; Ramires, Felix José Alvarez; Alves, Silvia Marinho Martins; Montera, Marcelo Westerlund; Lopes, Renato Delascio; Oliveira Junior, Mucio Tavares de; Scolari, Fernando Luis; Avila, Walkiria Samuel; Canesin, Manoel Fernandes; Bocchi, Edimar Alcides; Bacal, Fernando; Moura, Lidia Zytynski; Saad, Eduardo Benchimol; Scanavacca, Mauricio Ibrahim; Valdigem, Bruno Pereira; Cano, Manuel Nicolas; Abizaid, Alexandre Antonio Cunha; Ribeiro, Henrique Barbosa; Lemos Neto, Pedro Alves; Ribeiro, Gustavo Calado de Aguiar; Jatene, Fabio Biscegli; Dias, Ricardo Ribeiro; Beck-da-Silva, Luis; Rohde, Luis Eduardo Paim; Bittencourt, Marcelo Imbroinise; Pereira, Alexandre da Costa; Krieger, José Eduardo; Villacorta Junior, Humberto; Martins, Wolney de Andrade; Figueiredo Neto, José Albuquerque de; Cardoso, Juliano Novaes; Pastore, Carlos Alberto; Jatene, Ieda Biscegli; Tanaka, Ana Cristina Sayuri; Hotta, Viviane Tiemi; Romano, Minna Moreira Dias; Albuquerque, Denilson Campos de; Mourilhe-Rocha, Ricardo; Hajjar, Ludhmila Abrahão; Brito Junior, Fabio Sandoli de; Caramelli, Bruno; Calderaro, Daniela; Farsky, Pedro Silvio; Colafranceschi, Alexandre Siciliano; Pinto, Ibraim Masciarelli Francisco; Vieira, Marcelo Luiz Campos; Danzmann, Luiz Claudio; Barberato, Silvio Henrique; Mady, Charles; Martinelli Filho, Martino; Torbey, Ana Flavia Malheiros; Schwartzmann, Pedro Vellosa; Macedo, Ariane Vieira Scarlatelli; Ferreira, Silvia Moreira Ayub; Schmidt, Andre; Melo, Marcelo Dantas Tavares de; Lima Filho, Moysés Oliveira; Sposito, Andrei C; Brito, Flávio de Souza; Biolo, Andreia; Madrini Junior, Vagner; Rizk, Stephanie Itala; Mesquita, Evandro Tinoco.
Arq. bras. cardiol ; 121(7): e202400415, jun.2024. ilus, tab
Artigo em Português | CONASS, Sec. Est. Saúde SP, SESSP-IDPCPROD, Sec. Est. Saúde SP | ID: biblio-1556404

Assuntos
Diagnóstico
5.
J Thromb Thrombolysis ; 57(6): 1031-1039, 2024 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-38762708

RESUMO

Therapeutic anticoagulation showed inconsistent results in hospitalized patients with COVID-19 and selection of the best patients to use this strategy still a challenge balancing the risk of thrombotic and hemorrhagic outcomes. The present post-hoc analysis of the ACTION trial evaluated the variables independently associated with both bleeding events (major bleeding or clinically relevant non-major bleeding) and the composite outcomes thrombotic events (venous thromboembolism, myocardial infarction, stroke, systemic embolism, or major adverse limb events). Variables were assessed one by one with independent logistic regressions and final models were chosen based on Akaike information criteria. The model for bleeding events showed an area under the curve of 0.63 (95% confidence interval [CI] 0.53 to 0.73), while the model for thrombotic events had an area under the curve of 0.72 (95% CI 0.65 to 0.79). Non-invasive respiratory support was associated with thrombotic but not bleeding events, while invasive ventilation was associated with both outcomes (Odds Ratio of 7.03 [95 CI% 1.95 to 25.18] for thrombotic and 3.14 [95% CI 1.11 to 8.84] for bleeding events). Beyond respiratory support, creatinine level (Odds Ratio [OR] 1.01 95% CI 1.00 to 1.02 for every 1.0 mg/dL) and history of coronary disease (OR 3.67; 95% CI 1.32 to 10.29) were also independently associated to the risk of thrombotic events. Non-invasive respiratory support, history of coronary disease, and creatinine level may help to identify hospitalized COVID-19 patients at higher risk of thrombotic complications.ClinicalTrials.gov: NCT04394377.


Assuntos
COVID-19 , Produtos de Degradação da Fibrina e do Fibrinogênio , Hemorragia , Trombose , Humanos , COVID-19/sangue , COVID-19/complicações , COVID-19/diagnóstico , Produtos de Degradação da Fibrina e do Fibrinogênio/análise , Produtos de Degradação da Fibrina e do Fibrinogênio/metabolismo , Hemorragia/sangue , Hemorragia/diagnóstico , Hemorragia/etiologia , Hemorragia/induzido quimicamente , Masculino , Feminino , Trombose/sangue , Trombose/etiologia , Trombose/diagnóstico , Idoso , Pessoa de Meia-Idade , Hospitalização , Fatores de Risco , SARS-CoV-2 , Anticoagulantes/uso terapêutico , Anticoagulantes/efeitos adversos
6.
Int. j. cardiovasc. sci. (Impr.) ; 37(suppl.1): 17-17, abr. 2024.
Artigo em Português | CONASS, Sec. Est. Saúde SP, SESSP-IDPCPROD, Sec. Est. Saúde SP | ID: biblio-1538231

RESUMO

INTRODUÇÃO: A amiloidose transtiretina (ATTR) é uma doença multissistêmica causada pela deposição de proteína fibrilar em órgãos e tecidos. Os genótipos e fenótipos da ATTR são altamente heterogêneos. MÉTODOS: Apresentamos dados sobre sinais e sintomas físicos, avaliações cardíacas e neurológicas, e genética em pacientes incluídos no Registro de Amiloidose Cardíaca Transtiretina no Estado de São Paulo (REACT-SP), Brasil. RESULTADOS: Foram incluídos 644 pacientes, sendo 505 com a forma variante (ATTRv) e 139 com a forma selvagem (ATTRwt). Dezesseis mutações diferentes foram detectadas, sendo as mais comuns Val50Met (48,3%) e V142Ile (40,8%). No geral, mais da metade dos pacientes apresentou envolvimento cardíaco, e a diferença nessa proporção entre os grupos ATTRv e ATTRwt foi significativa (43,9 vs. 89,9%; p<0,001). O fenótipo neurológico também diferiu entre ATTRv e ATTRwt (56,8 vs. 31,7%; p<0,001). O fenótipo misto foi encontrado em 25,6% da população, sem diferença significativa entre as formas de amiloidose. Um grupo de pacientes permaneceu assintomático (10,4%), com uma proporção menor de pacientes assintomáticos no grupo ATTRwt. CONCLUSÕES: Este estudo detalha o espectro clínico e genético de pacientes com ATTR em São Paulo, Brasil. Esta análise preliminar destaca a considerável heterogeneidade fenotípica das manifestações neurológicas e cardíacas em pacientes com ATTR variante e ATTR do tipo selvagem.


Assuntos
Pré-Albumina , Amiloidose Familiar , Sinais e Sintomas , Perfil Genético
7.
JCO Glob Oncol ; 10: e2300484, 2024 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-38603658

RESUMO

PURPOSE: Cyclin inhibitors plus endocrine therapy represent the reference standard for hormone receptor-positive (HR+)/human epidermal growth factor receptor 2-negative (HER2-) locally advanced or metastatic breast cancer (ABC). Efficacy results on hard end points such as overall survival come from well-designed randomized clinical trials (RCTs). However, a limitation of RCTs is the low external results validity, and their extrapolation to a broader population may not be appropriate. Real-world studies can overcome these limitations, also increasing the reliability of RCTs. MATERIALS AND METHODS: The BrasiLEEira was an observational, longitudinal, retrospective, multicenter study to evaluate the effectiveness and safety of ribociclib plus nonsteroidal aromatase inhibitors in Brazilian women age 18 years or older with HR+/HER2- ABC. The study was approved by the institutional review boards of all 11 hospitals. Data were collected anonymously from medical records using an electronic case report form designed by an independent academic research organization, which conducted the study considering all recommendations of international guidelines. The primary end point was 1-year progression-free survival (PFS) rate. Secondary end points included mortality, dose reduction, and safety. RESULTS: The mean age of 76 patients was 57 years, and 28.9% were Black/Brown. The most prevalent comorbidity was arterial hypertension (34.7%). About 26.0% had endocrine-resistant disease, and 54.1% had more than three metastatic sites. The PFS rate was 77.6%. Three patients died (3.9%). Dose reductions occurred in 37.7% of patients. The most common adverse event was neutropenia (68.4%). CONCLUSION: The high-quality evidence from the BrasiLEEira study corroborates the RCTs' findings, expanding its validity to a broader spectrum and underrepresented population who may benefit from ribociclib treatment.


Assuntos
Inibidores da Aromatase , Neoplasias da Mama , Purinas , Feminino , Humanos , Aminopiridinas/efeitos adversos , Inibidores da Aromatase/efeitos adversos , Neoplasias da Mama/tratamento farmacológico , Neoplasias da Mama/patologia , Pessoa de Meia-Idade
9.
Arq Bras Cardiol ; 120(7): e20230303, 2023 08 04.
Artigo em Inglês, Português | MEDLINE | ID: mdl-37556656
10.
Oliveira, Gláucia Maria Moraes de; Almeida, Maria Cristina Costa de; Rassi, Daniela do Carmo; Bragança, Érika Olivier Vilela; Moura, Lidia Zytynski; Arrais, Magaly; Campos, Milena dos Santos Barros; Lemke, Viviana Guzzo; Avila, Walkiria Samuel; Lucena, Alexandre Jorge Gomes de; Almeida, André Luiz Cerqueira de; Brandão, Andréa Araujo; Ferreira, Andrea Dumsch de Aragon; Biolo, Andreia; Macedo, Ariane Vieira Scarlatelli; Falcão, Breno de Alencar Araripe; Polanczyk, Carisi Anne; Lantieri, Carla Janice Baister; Marques-Santos, Celi; Freire, Claudia Maria Vilas; Pellegrini, Denise; Alexandre, Elizabeth Regina Giunco; Braga, Fabiana Goulart Marcondes; Oliveira, Fabiana Michelle Feitosa de; Cintra, Fatima Dumas; Costa, Isabela Bispo Santos da Silva; Silva, José Sérgio Nascimento; Carreira, Lara Terra F; Magalhães, Lucelia Batista Neves Cunha; Matos, Luciana Diniz Nagem Janot de; Assad, Marcelo Heitor Vieira; Barbosa, Marcia M; Silva, Marconi Gomes da; Rivera, Maria Alayde Mendonça; Izar, Maria Cristina de Oliveira; Costa, Maria Elizabeth Navegantes Caetano; Paiva, Maria Sanali Moura de Oliveira; Castro, Marildes Luiza de; Uellendahl, Marly; Oliveira Junior, Mucio Tavares de; Souza, Olga Ferreira de; Costa, Ricardo Alves da; Coutinho, Ricardo Quental; Silva, Sheyla Cristina Tonheiro Ferro da; Martins, Sílvia Marinho; Brandão, Simone Cristina Soares; Buglia, Susimeire; Barbosa, Tatiana Maia Jorge de Ulhôa; Nascimento, Thais Aguiar do; Vieira, Thais; Campagnucci, Valquíria Pelisser; Chagas, Antonio Carlos Palandri.
Arq. bras. cardiol ; 120(7): e20230303, 2023. tab, graf
Artigo em Português | LILACS-Express | LILACS, CONASS, Sec. Est. Saúde SP, SESSP-IDPCPROD, Sec. Est. Saúde SP | ID: biblio-1447312
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